Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024:2742:131-149.
doi: 10.1007/978-1-0716-3561-2_11.

Establishing a Zebrafish Model for Borrelia burgdorferi Infection Using Immersion and Microinjection Methods

Affiliations

Establishing a Zebrafish Model for Borrelia burgdorferi Infection Using Immersion and Microinjection Methods

Erica Misner et al. Methods Mol Biol. 2024.

Abstract

Borrelia burgdorferi is the spirochetal bacterium that causes Lyme disease. Even though antimicrobial sensitivity of B. burgdorferi has been widely studied, there is still a need to develop an affordable, practical, high-throughput in vivo model which can be used to find effective antibiotic therapies, especially for the recently discovered persister and biofilm forms. Here, we describe the immersion and microinjection methods to introduce B. burgdorferi spirochetes into zebrafish larvae. The B. burgdorferi-zebrafish model can be produced by immersing 5-day post-fertilization (dpf) zebrafish in a B. burgdorferi culture, or by injecting B. burgdorferi into the hindbrain of zebrafish at 28 h post-fertilization (hpf). To demonstrate that B. burgdorferi indeed infect the fish, nested polymerase chain reaction (PCR), reverse transcription PCR (RT-PCR), live fluorescence imaging, histological staining, and wholemount immunohistochemical (IHC) methods can be used on B. burgdorferi-infected zebrafish.

Keywords: Borrelia burgdorferi; Genomic amplification; Immersion infection; Immunohistochemistry; Microinjection infection; Zebrafish model.

PubMed Disclaimer

References

    1. Sullivan C, Kim CH (2008) Zebrafish as a model for infectious disease and immune function. Fish Shellfish Immunol 25(4):341–350. https://doi.org/10.1016/j.fsi.2008.05.005 - DOI - PubMed
    1. Higginson EE, Simon R, Tennant SM (2016) Animal models for salmonellosis: applications in vaccine research. Clin Vaccine Immunol 23(9):746–756. https://doi.org/10.1128/CVI.00258-16 - DOI - PubMed - PMC
    1. Gencturk E, Mutlu S, Ulgen KO (2017) Advances in microfluidic devices made from thermoplastics used in cell biology and analyses. Biomicrofluidics 11(5):051502. https://doi.org/10.1063/1.4998604 - DOI - PubMed - PMC
    1. Jim KK, Engelen-Lee JY, van der Sar AM et al (2016) Infection of zebrafish embryos with live fluorescent Streptococcus pneumoniae as a real-time pneumococcal meningitis model. J Neuroinflammation 3(1):188. https://doi.org/10.1186/s12974-016-0655-y
    1. Goldsmith JR, Jobin C (2012) Think small: Zebrafish as a model system of human pathology. J Biomed Biotechnol 2012:817341. https://doi.org/10.1155/2012/817341 - DOI - PubMed - PMC

LinkOut - more resources